150
Participants
Start Date
July 26, 2019
Primary Completion Date
June 30, 2024
Study Completion Date
December 30, 2024
ChemoID Assay
"The ChemoID test is a CLIA-certified and CAP-accredited drug response assay performed by a hospital clinical pathology laboratory that uses patient's live tumor cells to indicate which chemotherapy agent (or combinations) will kill bulk of tumor cells, and cancer stem cells (CSCs) that are known to cause cancer to recur. During the assay, cancer stem cells and bulk tumor cells from an individual patient are exposed to FDA-approved chemotherapy drugs.~The test measures the cytotoxic effect of actual doses of standard-of-care chemotherapies. The ChemoID drug response assay reports a prioritized list of effective and ineffective chemotherapies. The test is designed to target cancer stem cells to mitigate tumor relapse."
Standard Chemotherapy
"Control chemotherapy treatment will be chosen from any of the following standard-of-care chemotherapy drugs or combinations:~Liposomal Doxorubicin; Docetaxel; Paclitaxel; Carboplatin; Cisplatin; Gemcitabine; Topotecan; Carboplatin, Gemcitabine; Cisplatin, Gemcitabine; Carboplatin, Liposomal Doxorubicin; Carboplatin, Paclitaxel; Carboplatin, Docetaxel. The treating physician will NOT receive the ChemoID assay results from the ChemoID lab."
West Penn Hospital, Allegheny Health Network, Pittsburgh
Charleston Area Medical Center (CAMC), Charleston
Edwards Comprehensive Cancer Center - Cabell Huntington Hospital, Huntington
Miami Cancer Institute/Baptist Health South Florida, Miami
University of Cincinnati Cancer Institute, Cincinnati
LSU Health Sciences Center, New Orleans
University of Oklahoma Health Sciences Center, Oklahoma City
Kaiser Permanente, Los Angeles
Cordgenics, LLC
INDUSTRY